Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia
Abstract Tumor lysis syndrome (TLS) is a common and fatal complication of childhood hematologic malignancies, especially acute lymphoblastic leukemia (ALL). The clinical features, therapeutic regimens, and outcomes of TLS have not been comprehensively analyzed in Chinese children with ALL. A total o...
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Nature Publishing Group
2021-05-01
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Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-021-88912-2 |
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doaj-395a3d2f1711449b903e2f29b15549cc |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yao Xue Jing Chen Siyuan Gao Xiaowen Zhai Ningling Wang Ju Gao Yu Lv Mengmeng Yin Yong Zhuang Hui Zhang Xiaofan Zhu Xuedong Wu Chi Kong Li Shaoyan Hu Changda Liang Runming Jin Hui Jiang Minghua Yang Lirong Sun Kaili Pan Jiaoyang Cai Jingyan Tang Xianmin Guan Yongjun Fang |
spellingShingle |
Yao Xue Jing Chen Siyuan Gao Xiaowen Zhai Ningling Wang Ju Gao Yu Lv Mengmeng Yin Yong Zhuang Hui Zhang Xiaofan Zhu Xuedong Wu Chi Kong Li Shaoyan Hu Changda Liang Runming Jin Hui Jiang Minghua Yang Lirong Sun Kaili Pan Jiaoyang Cai Jingyan Tang Xianmin Guan Yongjun Fang Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia Scientific Reports |
author_facet |
Yao Xue Jing Chen Siyuan Gao Xiaowen Zhai Ningling Wang Ju Gao Yu Lv Mengmeng Yin Yong Zhuang Hui Zhang Xiaofan Zhu Xuedong Wu Chi Kong Li Shaoyan Hu Changda Liang Runming Jin Hui Jiang Minghua Yang Lirong Sun Kaili Pan Jiaoyang Cai Jingyan Tang Xianmin Guan Yongjun Fang |
author_sort |
Yao Xue |
title |
Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia |
title_short |
Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia |
title_full |
Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia |
title_fullStr |
Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia |
title_full_unstemmed |
Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia |
title_sort |
clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemia |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-05-01 |
description |
Abstract Tumor lysis syndrome (TLS) is a common and fatal complication of childhood hematologic malignancies, especially acute lymphoblastic leukemia (ALL). The clinical features, therapeutic regimens, and outcomes of TLS have not been comprehensively analyzed in Chinese children with ALL. A total of 5537 children with ALL were recruited from the Chinese Children’s Cancer Group, including 79 diagnosed with TLS. The clinical characteristics, treatment regimens, and survival of TLS patients were analyzed. Age distribution of children with TLS was remarkably different from those without TLS. White blood cells (WBC) count ≥ 50 × 109/L was associated with a higher risk of TLS [odds ratio (OR) = 2.6, 95% CI = 1.6–4.5]. The incidence of T-ALL in TLS children was significantly higher than that in non-TLS controls (OR = 4.7, 95% CI = 2.6–8.8). Hyperphosphatemia and hypocalcemia were more common in TLS children with hyperleukocytosis (OR = 2.6, 95% CI = 1.0–6.9 and OR = 5.4, 95% CI = 2.0–14.2, respectively). Significant differences in levels of potassium (P = 0.004), calcium (P < 0.001), phosphorus (P < 0.001) and uric acid (P < 0.001) were observed between groups of TLS patients with and without increased creatinine. Laboratory analysis showed that older age was associated with a higher level of creatinine. Calcium level was notably lower in males. WBC count, lactate dehydrogenase, and creatinine levels were significantly higher in T-ALL subgroup, whereas procalcitonin level was higher in B-ALL children. Older age, infant, a higher level of WBC and T-ALL were risk factors TLS occurrence. Hyperleukocytosis has an impact on the severity of TLS, while renal injury may be an important feature in the process of TLS. |
url |
https://doi.org/10.1038/s41598-021-88912-2 |
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doaj-395a3d2f1711449b903e2f29b15549cc2021-05-09T11:33:04ZengNature Publishing GroupScientific Reports2045-23222021-05-011111910.1038/s41598-021-88912-2Clinical characteristics of tumor lysis syndrome in childhood acute lymphoblastic leukemiaYao Xue0Jing Chen1Siyuan Gao2Xiaowen Zhai3Ningling Wang4Ju Gao5Yu Lv6Mengmeng Yin7Yong Zhuang8Hui Zhang9Xiaofan Zhu10Xuedong Wu11Chi Kong Li12Shaoyan Hu13Changda Liang14Runming Jin15Hui Jiang16Minghua Yang17Lirong Sun18Kaili Pan19Jiaoyang Cai20Jingyan Tang21Xianmin Guan22Yongjun Fang23Department of Hematology and Oncology, Children’s Hospital of Nanjing Medical UniversityDepartment of Hematology/Oncology, Shanghai Children’s Medical Center, National Health Committee Key Laboratory of Pediatric Hematology & Oncology, School of Medicine, Shanghai Jiao Tong UniversityDepartment of Hematology and Oncology, Children’s Hospital of Nanjing Medical UniversityHematology Department, Children’s Hospital of Fudan UniversityDepartment of Pediatric, The Second Hospital of Anhui Medical UniversityDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Key Laboratory of Birth Defects and Related Disease of Women and Children, Ministry of EducationDepartment of Hematology, Kunming Children’s HospitalDepartment of Pediatric Hematology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Pediatrics, Qilu Hospital of Shandong UniversityDepartment of Hematology and Oncology, Guangzhou Women and Children’s Medical CenterState Key Laboratory of Experimental Hematology and Division of Pediatric Blood Diseases Center, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeDepartment of Pediatrics, Nanfang Hospital, Southern Medical UniversityDepartment of Pediatrics, Hong Kong Children’s Hospital, The Chinese University of Hong KongDepartment of Hematology/Oncology, Children’s Hospital of Soochow UniversityDepartment of Hematology/Oncology, Jiangxi Provincial Children’s HospitalDepartment of Pediatrics, Union Hospital of Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Hematology/Oncology, Shanghai Children’s Hospital, Shanghai Jiao Tong UniversityDepartment of Pediatrics, Xiangya Hospital Central South UniversityDepartment of Pediatrics, Affiliated Hospital of Qingdao UniversityDepartment of Hematology/Oncology, Northwest Women’s and Children’s HospitalDepartment of Hematology/Oncology, Shanghai Children’s Medical Center, National Health Committee Key Laboratory of Pediatric Hematology & Oncology, School of Medicine, Shanghai Jiao Tong UniversityDepartment of Hematology/Oncology, Shanghai Children’s Medical Center, National Health Committee Key Laboratory of Pediatric Hematology & Oncology, School of Medicine, Shanghai Jiao Tong UniversityDepartment of Hematology/Oncology, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, Children’s Hospital of Chongqing Medical UniversityDepartment of Hematology and Oncology, Children’s Hospital of Nanjing Medical UniversityAbstract Tumor lysis syndrome (TLS) is a common and fatal complication of childhood hematologic malignancies, especially acute lymphoblastic leukemia (ALL). The clinical features, therapeutic regimens, and outcomes of TLS have not been comprehensively analyzed in Chinese children with ALL. A total of 5537 children with ALL were recruited from the Chinese Children’s Cancer Group, including 79 diagnosed with TLS. The clinical characteristics, treatment regimens, and survival of TLS patients were analyzed. Age distribution of children with TLS was remarkably different from those without TLS. White blood cells (WBC) count ≥ 50 × 109/L was associated with a higher risk of TLS [odds ratio (OR) = 2.6, 95% CI = 1.6–4.5]. The incidence of T-ALL in TLS children was significantly higher than that in non-TLS controls (OR = 4.7, 95% CI = 2.6–8.8). Hyperphosphatemia and hypocalcemia were more common in TLS children with hyperleukocytosis (OR = 2.6, 95% CI = 1.0–6.9 and OR = 5.4, 95% CI = 2.0–14.2, respectively). Significant differences in levels of potassium (P = 0.004), calcium (P < 0.001), phosphorus (P < 0.001) and uric acid (P < 0.001) were observed between groups of TLS patients with and without increased creatinine. Laboratory analysis showed that older age was associated with a higher level of creatinine. Calcium level was notably lower in males. WBC count, lactate dehydrogenase, and creatinine levels were significantly higher in T-ALL subgroup, whereas procalcitonin level was higher in B-ALL children. Older age, infant, a higher level of WBC and T-ALL were risk factors TLS occurrence. Hyperleukocytosis has an impact on the severity of TLS, while renal injury may be an important feature in the process of TLS.https://doi.org/10.1038/s41598-021-88912-2 |